甘蓝型油菜BnFAD8基因编码序列的克隆和表达谱分析  

Cloning and expression characteristics of fatty acid desaturase 8 gene from rape (Brassica napus L.)

作　　者：刘绵学[1] 王茂华[1] 向俊蓓[1] 杨毅[1] 李旭锋[1] 

机构地区：[1]四川大学生命科学学院生物资源与生态环境教育部重点实验室,成都610064

出　　处：《四川大学学报（自然科学版）》2011年第3期697-702,共6页Journal of Sichuan University(Natural Science Edition)

基　　金：国家自然科学基金(30471095)

摘　　要：通过比对拟南芥等同源基因,克隆了甘蓝型油菜FAD8基因中的保守序列.以得到的FAD8(Fatty Acid Desaturase 8)保守序列片段为信息探针,在GenBank的EST数据库中检索高度同源的EST,并通过人工拼接及RT-PCR得到油菜该基因的全长为1299 bp的cDNA序列,命名为BnFAD8.序列分析结果中发现该基因符合质体定位的ω3脂肪酸脱饱和酶序列特征.通过比较22℃和8℃处理的甘蓝型油菜的BnFAD8基因表达谱,发现该基因在常温下仅存在痕量表达;而在低温条件下在叶中表达出现较大幅度的升高.推测BnFAD8基因和油菜的低温调控存在联系.Brassica napus fatty acid desaturase 8 （FADS） belongs to cold-induced omega 3 fatty acid desaturase. By aligning Arabidopsis FAD8 and other homologous FAD8 genes, one highly conserved sequence of FAD8 from rape was cloned in study. Using the FAD8 conserved sequence as a querying probe, highly homologous EST were obtained from database of GenBank and a putative complete ORF of 1299 bp （named. BnFAD8） was assembled according to the rape clone. Furthermore, the full length cDNA of Brassica napus FAD8 was cloned by RT-PCR with two primers designed based on this assembled cDNA sequence. Features of plasmid-located 0o3 fatty acid desaturase were found in sequence analy- sis of cDNA cloned. As shown in expression profile result, BnFAD8 was highly expressed in leaves at 8 ℃, but only trace-level expression in leaves at 22 ℃, which suggested that BnFAD8 involved in the process of rape cold acclimation.

关 键 词：甘蓝型油菜 基因克隆 BnFAD8 低温诱导表达 

分 类 号：Q78[生物学—分子生物学]